VOLUME 38 | ISSUE 3 | MAY-JUNE 2018

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A novel high-resolution melting analysis approach for rapid detection of vancomycin-resistant enterococci

Hani Adnan Ozbak

From the Department of Clinical Laboratory Sciences, Faculty of Applied Medical Sciences, Taibah University, Madinah, Saudi Arabia

How to cite this article:

Ozbak HA. Development of a novel high-resolution melting analysis approach for rapid detection of vancomycin-resistant enterococci. Ann Saudi Med 2018; 38(3): 200-207.

DOI: 10.5144/0256-4947.2018.200

Abstract

BACKGROUND: Vancomycin-resistant enterococci (VRE) are resistant to most classes of antibiotics. Diagnosis of VRE using standard methods takes 2 to 5 days. Development of a rapid PCR-assay that detects and identifies resistant genes in bacteria would provide time-critical information on the presence of VRE in clinical samples allowing early treatment and management of infected patients.

 

OBJECTIVES: Investigate the use of high resolution melting analysis (HRMA) and 16S-rRNA-PCR approach for rapid and cost-effective identification of VRE. 

 

DESIGN: Descriptive antibiotic susceptibility studies.

 

SETTING: Manchester Academic Health Sciences Centre and School of Translational Medicine, University of Manchester, UK, and Department of Clinical Laboratory Sciences, Taibah University, Saudi Arabia. 

 

MATERIALS AND METHODS: PCR-HRMA using 16S-rRNA V1-primers was used to detect and identify VRE. DNA from different strains of vancomycin-resistant and -sensitive Enterococcus faecalis (VSE) and Enterococcus faecium were amplified using V1-primer followed by HRMA in a single run. Differentiation of VRE from VSE was based on curve shapes generated against reference organisms (Bacteroides fragilis). 

 

MAIN OUTCOMES MEASURES: Amplification curves and difference plots for VRE and VSE.

 

RESULTS: Difference plots were generated for all vancomycin-resistant and -sensitive E faecalis and E faecium strains by subtracting their fluo.rescence melting profile from that of a reference-species B fragilis. A characteristic curve shape was produced by vancomycin-sensitive E faecalis and E faecium. However, vancomycin-resistant strains of these bacteria were associated with a markedly different curve shape facilitating a clear differentiation.

 

CONCLUSION: The 16S-PCR-HRMA approach has the potential for detecting vancomycin-resistant E faecium and E faecalis. Data with VRE provide the basis for combining VRE identification with pathogens speciation in a rapid, cheap assay able to identify a pathogen as an Enterococcus and whether it is vancomycin-sensitive or -resistant E faecium or E faecalis in a single PCR and HRMA run.

 

LIMITATIONS: Tested on specific, but not all, reference Enterococcus species and clinical isolates. 

 

CONFLICT OF INTEREST: None.

 

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